A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18067591



Internal ID20634632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:40865300..40876354hg38UCSC Ensembl
chr20:39493940..39504994hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3811055
hg1911055
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6537982
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18067591
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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